Welcome to the Ask the Doctor forum of our Association, here you have the opportunity to ask questions about any aspect of Peyronie’s Disease, and have those questions answered by Dr. Laurence Levine, Dr. John Mulhall and other members of our Medical Advisory Board or guest contributors They will provide you with an unbiased view of treatment and research information. Our physicians and guest contributors are considered leaders in the field of research and treatment of Peyronie's Disease. It is our goal to help you find answers and come to a better understanding of our common problem.

While the majority of medical professionals have knowledge of Peyronie’s Disease, the physicians who actually research and treat it comprehensively are few and far between and rarely speak out on public forums such as this one. The gap between comprehensive medical knowledge and the limited treatment options provided by less knowledgeable physicians frequently leave some men feeling angry and frustrated. Consequently many try to find their own cures; some seek treatment information from other sufferers with the disease and become willing to try what appears to have worked for them While sharing personal experience is important, applying those experiences with out knowledge of the possible consequences is often hazardous.

You may ask any question you wish, concerning Peyronie's Disease we receive many repeat questions on the same subject Due to the volume of questions submitted we edit identical subjects at the doctors' request so they may direct their answer to the subject matter.  We also receive many questions that contain personal histories and such requests for information will be edited to the actual question so we can give a more general answer to our readership. Previously addressed questions have been archived so you may look at them before you submit your personal concern, in doing so if your specific question still remains unanswered feel free to submit it.  You may also wish to look in our Topic section for more comprehensive information on Peyronie's disease

The questions and their answers may be posted monthly and we will do our best to answer 8-10 new questions per month depending upon physician availability.  Please be aware that our Doctors volunteer their time and expertise to help us do this and we need to be flexible to accommodate their busy schedules.

Honest questions deserve honest answers. The answered questions reflect each physician’s viewpoint and experience. Our physicians cannot answer some questions if the individual is asking for a diagnosis or personal treatment evaluation or recommendation online No responsible physician will diagnose or recommend treatment without personal contact Our Doctors' answers are informational only.

We urge you to participate in this Q&A, and to use our other general discussion forum to talk about the different subjects between yourselves One of the most devastating parts of this disease is the feeling of isolation it creates We hope that you will find answers and take the opportunity to talk with others who suffer from this disease